• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

样本中线粒体呼吸链酶活性的测量。

Measurement of mitochondrial respiratory chain enzymatic activities in samples.

机构信息

Department of Biomedical Sciences, University of Padova, Padova, Italy.

Veneto Institute of Molecular Medicine, Padova, Italy.

出版信息

STAR Protoc. 2022 Apr 15;3(2):101322. doi: 10.1016/j.xpro.2022.101322. eCollection 2022 Jun 17.

DOI:10.1016/j.xpro.2022.101322
PMID:35479112
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9036317/
Abstract

Mitochondrial respiratory chain (MRC) dysfunction is linked to mitochondrial disease as well as other common conditions such as diabetes, neurodegeneration, cancer, and aging. Thus, the evaluation of MRC enzymatic activities is fundamental for diagnostics and research purposes on experimental models. Here, we provide a verified and reliable protocol for mitochondria isolation from various samples and subsequent measurement of the activity of MRC complexes I-V plus citrate synthase (CS) through UV-VIS spectrophotometry. For complete details on the use and execution of this protocol, please refer to Brischigliaro et al. (2021).

摘要

线粒体呼吸链(MRC)功能障碍与线粒体疾病以及其他常见疾病有关,如糖尿病、神经退行性疾病、癌症和衰老。因此,评估 MRC 酶活性对于诊断和实验模型的研究目的至关重要。在这里,我们提供了一种经过验证和可靠的从各种样本中分离线粒体并通过紫外可见分光光度法测量 MRC 复合物 I-V 和柠檬酸合酶(CS)活性的方案。有关该方案使用和执行的完整详细信息,请参阅 Brischigliaro 等人(2021 年)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f1/9036317/1cecdaa4ca3b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f1/9036317/d6bea684ad49/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f1/9036317/1cecdaa4ca3b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f1/9036317/d6bea684ad49/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f1/9036317/1cecdaa4ca3b/gr1.jpg

相似文献

1
Measurement of mitochondrial respiratory chain enzymatic activities in samples.样本中线粒体呼吸链酶活性的测量。
STAR Protoc. 2022 Apr 15;3(2):101322. doi: 10.1016/j.xpro.2022.101322. eCollection 2022 Jun 17.
2
Structural rather than catalytic role for mitochondrial respiratory chain supercomplexes.线粒体呼吸链超级复合物的结构作用而非催化作用。
Elife. 2023 Oct 12;12:RP88084. doi: 10.7554/eLife.88084.
3
Age-associated decline in mitochondrial respiration and electron transport in Drosophila melanogaster.黑腹果蝇中线粒体呼吸和电子传递随年龄的下降。
Biochem J. 2005 Sep 1;390(Pt 2):501-11. doi: 10.1042/BJ20042130.
4
A Colorimetric Assay of Citrate Synthase Activity in Drosophila Melanogaster.黑腹果蝇中柠檬酸合酶活性的比色测定法。
J Vis Exp. 2020 Jan 16(155). doi: 10.3791/59454.
5
Changes in the respiratory chain complexes activities and in the mitochondrial DNA content during ageing in D. subobscura.暗果蝇衰老过程中呼吸链复合体活性及线粒体DNA含量的变化
Mech Ageing Dev. 1995 Oct 27;84(3):171-81. doi: 10.1016/0047-6374(95)01653-8.
6
Temperature-dependency of electron-transport activity in mitochondria with exogenous mitochondrial DNA in Drosophila.果蝇中外源线粒体DNA的线粒体电子传递活性的温度依赖性
Jpn J Genet. 1991 Jun;66(3):255-61. doi: 10.1266/jjg.66.255.
7
Pig Brain Mitochondria as a Biological Model for Study of Mitochondrial Respiration.猪脑线粒体作为研究线粒体呼吸的生物学模型
Folia Biol (Praha). 2016;62(1):15-25. doi: 10.14712/fb2016062010015.
8
Mitochondrial electron transport chain dysfunction during development does not extend lifespan in Drosophila melanogaster.发育过程中线粒体电子传递链功能障碍不会延长黑腹果蝇的寿命。
Mech Ageing Dev. 2010 Feb;131(2):156-64. doi: 10.1016/j.mad.2010.01.004. Epub 2010 Jan 22.
9
Biochemical analyses of the electron transport chain complexes by spectrophotometry.通过分光光度法对电子传递链复合物进行生化分析。
Methods Mol Biol. 2012;837:49-62. doi: 10.1007/978-1-61779-504-6_4.
10
Production of reactive oxygen species by the mitochondrial electron transport chain in Drosophila melanogaster.果蝇中线粒体电子传递链产生的活性氧物种。
J Bioenerg Biomembr. 2010 Apr;42(2):135-42. doi: 10.1007/s10863-010-9281-z. Epub 2010 Mar 19.

引用本文的文献

1
Mitochondrial hyper-acetylation induced by an engineered acetyltransferase promotes cellular senescence.由工程化乙酰转移酶诱导的线粒体高乙酰化促进细胞衰老。
iScience. 2025 Jul 29;28(9):113233. doi: 10.1016/j.isci.2025.113233. eCollection 2025 Sep 19.
2
Mitochondrial complex I deficiency occurs in skeletal muscle of a subgroup of individuals with Parkinson's disease.线粒体复合体I缺乏症发生在帕金森病患者亚组的骨骼肌中。
Commun Med (Lond). 2025 Apr 27;5(1):141. doi: 10.1038/s43856-025-00817-7.
3
Isolation of Intact Mitochondria From and Assessment of Mitochondrial Respiratory Capacity Using Seahorse Analyzer.

本文引用的文献

1
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster.在黑腹果蝇中模拟与 BCS1L 相关的人类线粒体疾病。
J Mol Med (Berl). 2021 Oct;99(10):1471-1485. doi: 10.1007/s00109-021-02110-1. Epub 2021 Jul 17.
2
Knockdown of Causes Cytochrome Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in .敲低[具体物质]会导致细胞色素氧化酶缺乏、神经肌肉损伤以及[具体物种]对氧化应激的抵抗力降低。
Front Physiol. 2019 Sep 6;10:1143. doi: 10.3389/fphys.2019.01143. eCollection 2019.
3
Feeding difficulties, a key feature of the NDUFS4 mitochondrial disease model.
从……中分离完整线粒体并使用海马分析仪评估线粒体呼吸能力
Bio Protoc. 2025 Feb 5;15(3):e5180. doi: 10.21769/BioProtoc.5180.
4
Effects of Atorvastatin and Simvastatin on the Bioenergetic Function of Isolated Rat Brain Mitochondria.阿托伐他汀和辛伐他汀对离体大鼠脑线粒体生物能量功能的影响。
Int J Mol Sci. 2024 Aug 3;25(15):8494. doi: 10.3390/ijms25158494.
5
Characterization of metabolic alterations in the lean metabolically unhealthy alpha defensin transgenic mice.瘦型代谢不健康α-防御素转基因小鼠代谢改变的特征分析
iScience. 2024 Jan 12;27(2):108802. doi: 10.1016/j.isci.2024.108802. eCollection 2024 Feb 16.
6
Structural rather than catalytic role for mitochondrial respiratory chain supercomplexes.线粒体呼吸链超级复合物的结构作用而非催化作用。
Elife. 2023 Oct 12;12:RP88084. doi: 10.7554/eLife.88084.
7
Drosophila Mpv17 forms an ion channel and regulates energy metabolism.果蝇Mpv17形成一个离子通道并调节能量代谢。
iScience. 2023 Sep 16;26(10):107955. doi: 10.1016/j.isci.2023.107955. eCollection 2023 Oct 20.
8
An Experimental Approach to Address the Functional Relationship between Antioxidant Enzymes and Mitochondrial Respiratory Complexes.一种研究抗氧化酶与线粒体呼吸复合体之间功能关系的实验方法。
Methods Protoc. 2023 Mar 24;6(2):32. doi: 10.3390/mps6020032.
9
Dysfunctional mitochondria accumulate in a skeletal muscle knockout model of Smn1, the causal gene of spinal muscular atrophy.在肌萎缩性脊髓侧索硬化症(SMA)的致病基因 Smn1 敲除的骨骼肌模型中,功能失调的线粒体积累。
Cell Death Dis. 2023 Feb 27;14(2):162. doi: 10.1038/s41419-023-05573-x.
10
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B.CG7630 是果蝇的细胞色素 c 氧化酶亚基 COX7B 的同源物。
EMBO Rep. 2022 Aug 3;23(8):e54825. doi: 10.15252/embr.202254825. Epub 2022 Jun 14.
喂养困难,是 NDUFS4 线粒体疾病模型的一个主要特征。
Dis Model Mech. 2018 Mar 27;11(3):dmm032482. doi: 10.1242/dmm.032482.
4
Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells.评估组织和培养细胞中线粒体呼吸链酶活性。
Nat Protoc. 2012 May 31;7(6):1235-46. doi: 10.1038/nprot.2012.058.
5
Assay of mitochondrial ATP synthesis in animal cells and tissues.动物细胞和组织中线粒体ATP合成的测定。
Methods Cell Biol. 2007;80:155-71. doi: 10.1016/S0091-679X(06)80007-5.
6
Biochemical assays of respiratory chain complex activity.呼吸链复合体活性的生化分析
Methods Cell Biol. 2007;80:93-119. doi: 10.1016/S0091-679X(06)80004-X.
7
Clinical and molecular findings in children with complex I deficiency.患有复合体I缺乏症儿童的临床和分子学发现。
Biochim Biophys Acta. 2004 Dec 6;1659(2-3):136-47. doi: 10.1016/j.bbabio.2004.09.006.
8
Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines.对患者肌肉活检样本、淋巴母细胞和转线粒体细胞系中线粒体氧化磷酸化的评估。
Methods Enzymol. 1996;264:484-509. doi: 10.1016/s0076-6879(96)64044-0.
9
Assay conditions for the mitochondrial NADH:coenzyme Q oxidoreductase.线粒体NADH:辅酶Q氧化还原酶的测定条件。
FEBS Lett. 1993 Oct 11;332(1-2):127-31. doi: 10.1016/0014-5793(93)80498-j.